Literature DB >> 1720562

Antigenic variation in Trypanosoma equiperdum.

C Roth1, C Jacquemot, C Giroud, F Bringaud, H Eisen, T Baltz.   

Abstract

Trypanosoma equiperdum is an African trypanosome that causes dourine in horses. Like the other African trypanosomes, T. equiperdum escapes elimination by the immune system of its host by using an elaborate system of antigenic variant. The trypanosomes are covered by a coat consisting of a single protein called the variable surface glycoprotein (VSG) that acts as the major trypanosome immunogen. As the host responds to one VSG, trypanosomes covered with another VSG become dominant. There is a loose order of appearance of these VSG during the infection. The factors that affect the timing of VSG expression and the effective size of the VSG repertoire in T. equiperdum are reviewed. The VSG genes are generally activated by a process of duplicative transposition involving the duplication of a silent VSG gene and inserting a copy of the gene into an expression site. The order of VSG expression is related to the amount of homology between the silent gene and the expression site. The genes expressed late in infection lack extensive homology with the expression site and depend on homology with the gene in the expression site. The genes coding for VSG expressed late in infection are hybrid genes because of this mode of transfer. This transfer mechanism allows the trypanosome to create complex VSG genes from parts of several different silent genes that are each pseudogenes. Additionally, data are presented showing that only a limited portion of the VSG is actually seen by the host immune system. These factors indicate that the effective VSG repertoire is greater than the number of VSG genes in the trypanosome genome.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1720562     DOI: 10.1016/0923-2508(91)90087-q

Source DB:  PubMed          Journal:  Res Microbiol        ISSN: 0923-2508            Impact factor:   3.992


  4 in total

Review 1.  Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections.

Authors:  K W Deitsch; E R Moxon; T E Wellems
Journal:  Microbiol Mol Biol Rev       Date:  1997-09       Impact factor: 11.056

2.  A lipopolysaccharide-binding domain of the Campylobacter fetus S-layer protein resides within the conserved N terminus of a family of silent and divergent homologs.

Authors:  J Dworkin; M K Tummuru; M J Blaser
Journal:  J Bacteriol       Date:  1995-04       Impact factor: 3.490

3.  Genomic analysis of Bacteroides fragilis reveals extensive DNA inversions regulating cell surface adaptation.

Authors:  Tomomi Kuwahara; Atsushi Yamashita; Hideki Hirakawa; Haruyuki Nakayama; Hidehiro Toh; Natsumi Okada; Satoru Kuhara; Masahira Hattori; Tetsuya Hayashi; Yoshinari Ohnishi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-04       Impact factor: 11.205

4.  Analysis of the VSG gene silent archive in Trypanosoma brucei reveals that mosaic gene expression is prominent in antigenic variation and is favored by archive substructure.

Authors:  Lucio Marcello; J David Barry
Journal:  Genome Res       Date:  2007-07-25       Impact factor: 9.043

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.